Submit or Track your Manuscript LOG-IN

Sublethal Dose Impact of λ Cyhalothrin on Life Table Parameters of Ladybird Beetle, Coccinella septempunctata (Coleoptera: Curculionidae) Reveals Tolerance in Field Population

PJZ_55_3_1393-1399

Sublethal Dose Impact of λ Cyhalothrin on Life Table Parameters of Ladybird Beetle, Coccinella septempunctata (Coleoptera: Curculionidae) Reveals Tolerance in Field Population

Muhammad Rizwan1*, Bilal Atta1, Muhammad Arshad2, Sohail Akhter3,

Muhammad Tahir3, Misbah Rizwan1, Muddassir Ali1 and Arshad Makhdoon Sabir1

1Rice Research Institute, Kala Shah Kaku, Punjab, Pakistan

2Department of Entomology, University of Sargodha, Sargodha 40100, Pakistan

3Department of Entomology, Faculty of Agricultural and Environmental Sciences, Islamia University of Bahawalpur, Bahawalpur, Pakistan

ABSTRACT

Insecticides are a quick tool to suppress insect pests and an important element of integrated pest management (IPM). λ cyhalothrin, a pyrethroid, is commonly used to manage economic insect pests in agricultural crops since long. An assay was designed to evaluate the efficacy of λ cyhalothrin on biological parameters of generalist predator, Coccinella septempunctata. Results indicated that λ cyhalothin has no significant impact on developmental life stages of larvae of ladybird beetle but it significantly reduced the span of total adult longevity (30.8 to 26.91 d), female adult longevity (31.5 to 27.79 d), and male adult longevity (29.4 to 25.56 d) as compared to control. Among population parameters, λ cyhalothin had a non-significant impact on adult preoviposition (APOP), total preoviposition period (TPOP), oviposition period, intrinsic rate of increase, finite rate of increase, and mean generation time (T). However, it had significantly reduced the fecundity of females from 294.00 to 262.43 eggs/female and net reproductive rate (R0) (174 to 91.85 d). Our results showed that C. septempunctata had adopted to manage λ cyhalothrin and it could be used in experiments involving C. septempunctata as a natural biocontrol agent.


Article Information

Received 25 September, 2020

Revised 26 October 2020

Accepted 20 November, 2020

Available online 02 June 2022

(early access)

Published 14 April 2023

Authors’ Contribution

Muhammad R, BA and Misbah R conducted the experiment, Muhammad R analyzed the data. Muhammad R, BA, Muhammad A, MT, SA and Muddassir A wrote the article. AMS critically reviewed and revised the manuscript.

Key words

Coccinella septempunctata, λ cyhalothrin, Generalist predator, Life table parameters, Sublethal dose

DOI: https://dx.doi.org/10.17582/journal.pjz/20200925080903

* Corresponding author: [email protected]

0030-9923/2023/0003-1393 $ 9.00/0

Copyright 2023 by the authors. Licensee Zoological Society of Pakistan.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).



INTRODUCTION

Ladybird beetles are the member of class insecta and belongs to the family Coccinellidae (Atta et al., 2019). The lady bird beetle (Coleoptera: Coccinellidae) is common to a wide range of natural and agricultural habitats with worldwide distribution. Coccinellids are Holometabolous insects possess four stages in their life cycle i.e., egg, larva, pupa, and adult. There are three molting and four larval instars (Pervez, 2004). All motile stages are predator but the larval and adult stages are very good predators of aphids and other small insects (Hangay and Zborowski, 2010). Its 3rd and 4th instars larvae are more voracious as compared to 1st and 2nd instar (Atta et al., 2019). Predatory potentials of females are more than males and laboratory reared adults are also more voracious than the field collected. Wheat (Triticum aestivum L.) is the main cereal staple crop of Pakistan and affected by aphids (Anonymous, 2018; Atta et al., 2019). Therefore, aphids attained the status of regular pest in Pakistan and regular monitoring of wheat crop is very important during the crop season (Abdulkhairova, 1979; Atta et al., 2019). Biological control is the action of parasitoids, predators and pathogens in maintaining density at a lower average than would otherwise occur. According to Sathe and Bhosale (2001), predators are the organism which directly attack, kill, and eat one of the other species (prey of host). Biological control agents comprises an important elements of many integrated pest management (IPM) program but many synthetic pesticides affect them negatively (Mordue and Blackwell, 1993). Natural enemies/ biological control agents are the most important factors to regulate the pest population for keeping the insect pests below economic threshold level (Atta et al., 2019). Ladybird beetles are very common for controlling many insects and different studies have been done on them (Singh and Bras, 2004; Ullah et al., 2012; Farooq et al., 2018; Atta et al., 2019). λ cyhalothrin is commonly used insecticides for insect pest management on wheat, rice, and other crops (Atta et al., 2019).

Arthropods resistance to insecticides is of great concern in integrated pest management programs for applied entomologist. More than 600 species of insects and mites have been reported to develop resistance to one or more chemicals (Whalon et al., 2012). The development of resistance in insect pests lower the agronomic value of the insecticides (Jiang et al., 2011Whalon et al., 2015). On the other hand, fewer insects from natural enemies have shown resistance to insecticides (Croft, 1990Whalon et al., 2012). The repeated exposure to same to pesticides can evolve resistance in natural enemies like agricultural insect pests (Croft and Morse, 1979Pathan et al., 2008Pree et al., 1989Rodrigues et al., 2013a). The development of resistance to certain pesticide could be attributed to intrinsic factors such as genetic makeup, behavioural patterns, and metabolic physiology, in addition to extrinsic factors such as pesticide properties and exposure frequency and coverage (Forgash, 1984Georghiou and Taylor, 1977aRosenheim and Tabashnik, 1990WHO, 1957). It is therefore of interest that certain predator insects appear less susceptible as compared to other insect/ groups (Tillman and Mulrooney, 2000Williams et al., 2003), their prey (Gesraha, 2007), or even key pest species (Spíndola et al., 2013).

To use beneficial arthropods as bio-control agents or preserve their local natural populations in integrated pest management, their susceptibility to the pesticides used must be taken into account. In order to save released or local beneficial fauna and to augment and exploit their performance, several well-known strategies needed to be exploited. Looking for preparations harmless to biological agents among the existing pesticides; developing novel selective active ingredients finding (collecting/selecting) tolerant or resistant strains of natural enemies. The success of biological control may be enhanced by preventing the careless use of pesticides by having direct and indirect toxic effects on natural enemies. These adverse effects on the bio-agents can be minimized by considering and implementing some tactics which may play important role in expanding the function of biological control. The goal of IPM is to select such chemicals that are having compatibility. So, this study had been carried out to evaluate the sublethal impact of λ cyhalothrin on biological parameters of ladybird beetle.

MATERIALS AND METHODS

Insects

Coccinella septempunctata adults were collected from experimental area Rice Research Institute Kala Shah Kaku, Pakistan during the season 2018. Adults collected were reared in laboratory and Aphis gossypii were supplied as diet on daily basis collected from field. One generation (F0) was reared in the laboratory. Forty-five eggs were used in this study for each treatment. Grubs were supplied with sufficient number of A. gossypii as food. 2nd stage in stars were introduced into treated petri dishes to record the impact of insecticide life table parameters.

Insecticide

λ cyhlothrin (Karate 5EC), a commercial product of Syngenta, Pakistan, was used for sublethal studies against C. septempunctata larvae for biological parameters studies. Stock solution of 0.1% ml/L was prepared in distilled water. Then further two dilutions were made viz., 0.05 and 0.025 ml/L. Central doses 0.05 ml/L was selected for sublethal studies. For control only distilled water was used.

Bioassay

15 ml of selected dose were poured in the perti dishes and then it was shaked for 10-15seconds so that dose may be distributed to entire surface of the flask. The remaining liquid was wasted and petri dish was kept in front of fan to let it dry. Distilled water was used for control treatment. 45 eggs were used in this study. Due to higher mortality of 1st instar, 2nd instar larvae were put inside petri dish. Data for life stage and mortality was collected after 12 h (0900 and 2100 h). Adults of the same treatment were sexed to record the fecundity and life span for each treatment till death of each individual.

Statistical analysis

The basic life table parameters such as age-stage survival rate (Sxj), reproductive value (Vxj), age-stage specific life expectancy rate (Exj), intrinsic rate of increase (r), reproductive rate (R0), Finite rate of increase (λ), and mean generation time (T), were analyzed using the computer program TWOSEX-MS Chart (Chi and Liu, 1985; Chi, 2016a, b). The standard errors were calculated using the bootstrap technique included in the program with 100,000 random sampling (Efron and Tibshirani, 1993). Adult longevity, adult pre-oviposition period (APOP), total pre-oviposition period (TPOP), fecundity and population parameters (r, λ, R0, and T) were compared using the paired bootstrap test based on the confidence interval of the differences. Survival rate and reproductive value curves were plotted using MS Word software-2013.

RESULTS AND DISCUSSION

Age-stage two sex life tables

The development duration for each stage of C. septumpunctata are presented in Table I. The development period was the shortest in λ cyhalothrin (33.52d) followed by control (33.6 d). Moreover, the females’ life periods were longer than males in both treatments. Adult male longevity decreased in λ cyhalothrin treatment (25.56 d) as compared to control (29.40). In the same way, female longevity and total adult longevity was significantly lower (27.79 d) and (26.91 d) for insecticide treated grubs as compared to control (31.5 d) and (30.80 d), respectively. Age-stage, two sex life tables parameters describes the probability of a new born to survive to specific age (x) and stage (j) (Figs. 1-3). The age-stage curve (Sxj) describes a higher survival rate on control as compared to treatment. The lx, fxj, and mx curves indicate that C. septempunctata had higher survival on control as compared to lamnda cyhalothrin. While the highest fecundity was recorded in control treatment as compared to sublethal dose of λ cyhalothrin.

 

Table I. Effect of λ cyhlothrin on duration of development of C. septumpunctata (days) reared on A. gossypi.

Development

stage

N

Control

N

λ cyhalothrin

Egg

45

5.00 ± 0.00 a

45

5.00 ± 0.00 a

L1

44

4.00 ± 0.00 a

43

4.00 ± 0.00 a

L2

40

5.10 ± 0.12 a

40

5.08 ± 0.12 a

L3

34

5.56 ± 0.20 a

33

5.61 ± 0.17 a

L4

30

6.53 ± 0.15 a

28

6.64 ± 0.15 a

Pupa

30

7.07 ± 0.15 a

23

7.17 ± 0.16 a

Preadult

30

33.6 ± 2.30a

23

33.52 ± 0.32 a

Adult longevity

30.80 ± 0.57 a

26.91 ± 0.63 b

Female

20

31.50 ± 0.60 a

14

27.79 ± 0.79 b

Male

10

29.40 ± 1.13 a

9

25.56 ± 0.88 b

 

SEs were estimated by bootstrapping (100,000 replications). N, number of individuals completing a specific stage.

 

Age stage specific life expectancy curves (Exj) were plotted in Figure 2. The newly hatched eggs of C. septempunctata were expected to survive for a longer period in control as compared to treated larvae. Both, males and females are expected to live a longer life when treated with distilled water as compared to λ cyhalothrin.

Age-stage-specific reproduction rate (Vxj) for different treatments plotted in Figure 3. Adult females contributed more to the population as they are the most productive stages of a population. Moreover, the successful adult emergence recorded more females as compared to males in all treatments. The highest age-stage reproductive value was recorded in control (1.1427) treatment, followed by λ cyhalothrin (1.1295). The fecundity of an individual is affected by the conditions in which it is raised. The fxj curve explains the highest fecundity in λ cyhalothrin treated individuals was 19.8 eggs/day at 40th day while in control peak value 17.8 eggs was recorded on 42th day (Fig. 4).

 

 

 

 

Population parameters

Population were recorded for control and sublethal dose of λ cyhalothin insecticide. SEs were estimated with bootstrap technique with 100,000 replicatons. Net Reproductive rate (R0) was highest for control (147.00) followed by λ cyhalothin (91.85). Intrinsic rate of increase (r) was maximum for control (0.1339) followed by λ cyhalothin (0.1218). Mean generation time (T) was maximum for control (37.41) followed by λ cyhalothin (37.13) but statistically insignificant. Finite rate of increase (λ) values were highest to lowest for control (1.1427) as compared to λ cyhalothin (1.1295) (Table II).

 

Table II. Effect of λ cyhlothrin on fecundity and life table parameters (Mean ± SE) of C. septumpunctata reared on A. gossypi.

Parameters

Control

λ cyhalothrin

APOP

4.60 ± 0.11 a

4.14 ± 0.23 a

TPOP

29.20 ± 0.533 a

28.57 ± 0.40 a

Oviposition period

14.20 ± 0.2634 a

13.36 ± 0.41 a

Fecundity (eggs/female)

294.00 ± 5.835 a

262.43 ± 4.98 b

R0 (offspring individual-1)

147 ± 23.4808 a

91.85 ± 43.72 b

T (d)

45.41 ± 0.652 a

45.13 ± 0.365 a

r (d-1)

0.13387±0.0052a

0.1218±0.0066 a

λ (d-1)

1.14269±0.0059a

1.1295±0.0074a

 

APOP, adult pre-oviposition period; TPOP, total pre-oviposition period; R0, net reproductive rate; T, mean generation time; r, intrinsic rate of increase; λ, finite rate of increase. SEs were estimated by bootstrapping (100,000 replications).

 

DISCUSSION

IPM includes the integration of insecticides with other natural controlling agents such as predators, parasitoids, and parasites (Bilal et al., 2019), but it has been seldom achieved due to incompatibility of parts of IPM especially insecticides and biocontrol agents (Tabashnik and Johnson, 1999). Insecticides are found equally toxic to natural enemies (Bilal et al., 2019) and less toxicity to natural enemies other than pest is viewed as a rare exception (Croft, 1990). With the advancement in insect pests’ management techniques, insecticides are still primary tool for insect pest management. The impact of insecticides on beneficial fauna helping in pest management without an additional cost to IPM is an important matter (Atta et al., 2019) (Fig. 1).

λ cyhalothrin is a pyrethroid used on a wide scale for insect pest controlling programs. The results indicated that sublethal dose of λ cyhalothrin had a non-significant on developmental stages of ladybird beetle, however, pre-adult period was shorter than control. These results suggest development of tolerance in C. septempunctata against λ cyhalothrin, a pyrethroid. The development of resistance in coccinellid species field populations against λ cyhalothrin and pyrethroids was reported earlier by researchers in other countries (Torris et al., 2015; Rodrigues et al., 2013a, b). Bozsik (2006) reported that λ cyhalothrin is moderately harmful to C. septempunctata adults that is fairly similar to our results. The less survival of C. septempunctata as compared to the control might be attributed to the outbreak of aphids after pyrethoids application in field (Deguine et al., 2000; Godfrey et al., 2000) (Fig. 2).

λ cyhalothrin is among type-II pyrethroids which are more toxic due to presence of cyano group in molecule as compared to type-I pyrethroids such as permthrin and bifenthrin (Sattelle and Yamamoto, 1988; Khambay and Jewess, 2010; Torres et al., 2015). Wilis and Jepson (1994) reported the same for deltamethrin pyrethroid that C. septempunctata moved to lower parts of the shelter when exposed to deltamethrin. It may be due to that it had adopted to manage with the situation when exposed to λ cyhalothrin. Our results indicated that λ cyhalothrin had long term impact on C. septempunctata such as adult longevity of the male and female adult. This may be attributed to variable biological, operational, and genetic influences (Georghiou and Taylor, 1977a, b) (Fig. 3).

The sublethal application may have a suppressive or vice versa impact on fecundity of an insect. It means that it may reduce or augment its fecundity (Ali et al., 2017). The reduced fecundity of the female may be attributed to this factor. However, the population parameters such as generation time (T), intrinsic rate of increase (r), finite rate of increase (λ), and net reproductive rate were remained non-significant for control and λ cyhalothrin which may be attributed to development of resistance in field population of C. septempunctata against λ cyhalothrin. The development of resistance to an insecticide is not a permanent character in case of insects. An insect resistant to a certain insecticide may become susceptible again if raised in an insecticide free environment over generations (Ya-jun et al., 2014). The number of generations have not been reported for an insect for loss of resistance against an insecticide. This may be due to specific biology of an insect. The loss of resistance could be evaluated in the laboratory by producing a resistant biotype for a specific chemical. However, this evaluation may require an additional cost which depends on the biology of biocontrol agent under study (Fig. 4).

CONCLUSION

Our results revealed that C. septempunctata may have developed to manage λ cyhalothrin, and the insecticide may have not a significant damaging impact upon field population of ladybird beetle, C. septempunctata. It can be used in IPM programs involving C. septempunctata as a biological control agent.

Statement of conflict of interest

The authors have declared no conflict of interest.

REFERENCES

Abdulkhairova, S., 1979. The injuriousness of cereal aphids. Zashchita Rastenii, 10: 44.

Ali, E., Liao, X., Yang, P., Mao, K., Zhang, X., Shakeel, M., Salim, A.M.A., Wan, H. and Li, L., 2017. Sublethal effects of buprofezin on development and reproduction in the white-backed planthopper, Sogatella furcifera (Hemiptera: Delphacidae). Sci. Rep., 7: 16913. https://doi.org/10.1038/s41598-017-17190-8

Anonymous, 2018. Economic survey of Pakistan. Min. Food Agric., Fed. Bureau of Statistics, Islamabad, Pakistan

Atta, B., Rizwan, M., Sabir, A.M., Ayub, M.A., Akhter, M.F., Ayub, M.B. and Nadeem, S., 2019. Comparative incidence and abundance of aphids and their associated predators on canola in Pakistan. Pak. Entomol., 41: 174–152.

Bilal, M., Hussain, M., Umer, M., Ejaz, N., Noushahi, H.A., Atta, B. and Rizwan, M., 2019. Population incidence and efficacy of chemical control against rice leaffolder (Cnaphnalocrocis medinalis Guenee) (Pyralidae: Lepidoptera). Asian Pl. Res. J., 2: 1–7. https://doi.org/10.9734/aprj/2019/v2i230040

Bozsik, A., 2006. Susceptibility of adult Coccinella septempunctata (Coleoptera: Coccinellidae) to insecticides with different modes of action. J. Pest Manage. Sci., 62: 651–654. https://doi.org/10.1002/ps.1221

Chi, H. and Liu, H., 1985. Two new methods for the study of insect population ecology. Bull. Inst. Zool. Acad. Sin., 24: 225–240.

Chi, H., 2016a. Two Sex-MSChart: Computer program for age stage, two-sex life table analysis. http://140.120.197.173/ecology/

Chi, H., 2016b. Timing-MSChart: A computer program for the population projection based on age-stage, two-sex life table. http://140.120.197.173/Ecology/Download/TIMING-MSChart.rar (accessed 27 March 2020).

Croft, B.A. and Morse, J.G., 1979. Recent advances in natural enemy-pesticide research. Entomophaga24: 3–11. https://doi.org/10.1007/BF02377504

Croft, B.A., 1990. Pesticide resistance. Documentation. In: Arthropod biological control agents and pesticides (ed. B.A. Croft). John Wiley and Sons, New York, pp. 357–381.

Deguine, J.P., Goze, E. and Leclant, F., 2000. The consequences of late outbreaks of the aphid Aphis gossypii in cotton growing in Central Africa: Towards a possible method for the prevention of cotton stickness. Int. J. Pest Manage., 46: 86–89. https://doi.org/10.1080/096708700227426

Efron, B. and Tibshirani, R.J., 1993. An introduction to the bootstrap. J. Am. Stat. Assoc., 89: 436. https://doi.org/10.1007/978-1-4899-4541-9

Farooq, M., Shakeel, M., Iftikhar, A., Shahid, M.R. and Zhu, X., 2018. Age-stage, two-sex life tables of the lady beetle (Coleoptera: Coccinellidae) feeding on different aphid species. J. econ. Ent., 111: 575-585. https://doi.org/10.1093/jee/toy012

Forgash, A.J., 1984. History, evolution, and consequences of insecticide resistance. Pestic Biochem. Physiol., 22: 178–186. https://doi.org/10.1016/0048-3575(84)90087-7

Georghiou, G.P. and Taylor, C.E., 1977a. Genetic and biological influences in the evolution of insecticide resistance. J. econ. Ent., 70: 319–323. https://doi.org/10.1093/jee/70.3.319

Georghiou, G.P. and Taylor, C.E., 1977b. Operational influences in the evolution of insecticide resistance. J. econ. Ent., 70: 653–658. https://doi.org/10.1093/jee/70.5.653

Gesraha, M.A., 2007. Impact of some insecticides on the Coccinellid predator, Coccinella undecimpunctata L. and its aphid prey, Brevicoryne brassicae L. Egypt. J. Biol. Pest. Contr., 17: 65–69.

Godfrey, L., Rosenheim, J.A. and Goodell, P.B., 2000. Cotton aphid emerges as major pest in SJV cotton. Calif. Agric., 54: 26–29. https://doi.org/10.3733/ca.v054n06p26

Hangay, G. and Zborowski, P., 2010. A guide to the beetles of Australia. Csiro Publishing. https://doi.org/10.1071/9780643100121

Jiang, W., Guo, W., Lu, W., Shi, X., Xiong, M., Wang, Z. and Li, G., 2011. Target site insensitivity mutations in the AChE and LdVssc1 confer resistance to pyrethroids and carbamates in Leptinotarsa decemlineata in northern Xinjiang Uygur autonomous region. Pest. Biochem. Physiol., 100: 74-81.

Khambay, B.P.S. and Jewess, P.J., 2010. Pyrethroids. In: Insect control (eds. L.I. Gilbert and S.S. Gill). Academic Press, London, United Kingdom. pp. 1–34. https://doi.org/10.1016/B0-44-451924-6/00075-2

Mordue, A.J. and Blackwell, A., 1993. Azadirectin. An update. J. Insect Physiol., 39: 903–924. https://doi.org/10.1016/0022-1910(93)90001-8

Pathan, A.K., Sayyed, A.H., Aslam, M., Razaq, M., Jilani, G. and Saleem, M.A., 2008. Evidence of field-evolved resistance to organophosphates and pyrethroids in Chrysoperla carnea (Neuroptera: Chrysopidae). J. econ. Ent., 101: 1676–1684. https://doi.org/10.1603/0022-0493(2008)101[1676:EOFRTO]2.0.CO;2

Pervez, A., 2004. Predaceous coccinellids in India: Predatorprey catalogue. Ori. Insects, 38: 27-61. https://doi.org/10.1080/00305316.2004.10417373

Pree, D.J., Archibald, D.E. and Morrison, R.K., 1989. Resistance to insecticides in the common green lacewing Chrysoperla carnea (Neuroptera: Chrysopidae) in southern Ontario. J. econ. Ent., 82: 29–34. https://doi.org/10.1093/jee/82.1.29

Rodrigues, A.R.S., Spindola, A.F., Torres, J.B., Siqueira, H.A.A., Colares, F., 2013a. Response of different populations of seven lady beetle species to lambda-cyhalothrin with record of resistance. Ecotoxicol. Environ. Saf., 96: 53–60. https://doi.org/10.1016/j.ecoenv.2013.06.014

Rodrigues, A.R.S., Torres, J.B., Siqueira, H.A.A., Lacerda, D.P.A., 2013b. Inheritance of lambda-cyhalothrin resistance in the predator lady beetle Eriopis connexa (Germar) (Coleoptera: Coccinellidae). Biol. Contr., 64: 217–224. https://doi.org/10.1016/j.biocontrol.2012.11.018

Rosenheim, J.A. and Tabashnik, B.E., 1990. Evolution of pesticide resistance: interactions between generation time and genetic, ecological, and operational factors. J. econ. Ent., 83: 1184–1193. https://doi.org/10.1093/jee/83.4.1184

Sathe, T.V. and Bhosale, Y.A., 2001. Insect pest predators. Daya publishing house, Delhi, pp. 124.

Sattelle, D.B. and Yamamoto, D., 1988. Molecular targets of pyrethroid insecticides. Adv. Insect. Physiol., 20: 147–213. https://doi.org/10.1016/S0065-2806(08)60025-9

Singh, J. and Bras, K.S., 2004. Mass production and biological control potential of coccinellids in India. Indian insect predators in biological control. Edn Daya Publishing House, Delhi, India. pp. 204–260.

Spíndola, A.F., Silva-Torres, C.S.A., Rodrigues, A.R.S. and Torres, J.B., 2013. Survival and behavioural responses of the predatory ladybird beetle, Eriopis connexa populations susceptible and resistant to a pyrethroid insecticide. Bull. entomol. Res., 103: 485–494. https://doi.org/10.1017/S0007485313000072

Tabashnik, B.E. and Johnson, M.W., 1999. Evolution of pesticide resistance in natural enemies. In: Handbook of biological control (eds. T.S. Bellows and T.W. Fisher). Academic Press, New York, pp. 673–698. https://doi.org/10.1016/B978-012257305-7/50071-0

Tillman, P.G. and Mulrooney, J.E., 2000. Effect of selected insecticides on the natural enemies Coleomegilla maculata and Hippodamia convergens (Coleoptera: Coccinellidae), Geocoris punctipes (Hemiptera: Lygaeidae), and Bracon mellitor, Cardiochiles nigriceps, and Cotesia marginiventris (Hymenoptera: Braconidae) in cotton. J. econ. Ent., 93: 1638–1643. https://doi.org/10.1603/0022-0493-93.6.1638

Torres, J.B., Rodrigues, A.R.S., Barros, E.M. and Santos, D.S., 2015. λ Cyhalothrin resistance in the lady beetle eriopis connexa (Coleoptera: Coccinellidae) confers tolerance to other pyrethroids. J. econ. Ent., 108: 60–68. https://doi.org/10.1093/jee/tou035

Ullah, R., Haq, F., Ahmad, H., Inayatullah, M. and Saeed, K., 2012. Morphological characteristic of ladybird beetles collected from District DiLower, Pakistan. Afr. J. Biotechnol., 11: 9149–9155. https://doi.org/10.5897/AJB11.1363

Whalon, M.E., Mota-Sanchez, D., Hollingworth, R.M. and Duynslager, L., 2012. Arthropod pesticide resistance database. Available in (http://www.pesticideresistance.org/search/1). Accessed 22.05.2020

Whalon, M.E., Mota-Sanchez, D., Hollingworth, R.M. and Duynslager, L., 2015. Arthropod Pesticide Resistance Database. http://www.pesticideresistance.org/ (accessed 03.10.2020).

WHO, 1957. Expert committee on insecticides: Seventh report. Geneva, Tech. Rep. Ser., 125: 31.

Wilis, J.A. and Jepson, P.C., 1994. Sub-lethal effects of deltamethrin residues on the within-crop behavior and distribution of C. septempunctata. J. Ent. Exp. Appl., 72: 33–45. https://doi.org/10.1111/j.1570-7458.1994.tb01800.x

Williams, T., Valle, J. and Viñuela, E., 2003. Is the naturally derived insecticide Spinosad® compatible with insect natural enemies? Biocont. Sci. Tech., 13: 459–475. https://doi.org/10.1080/0958315031000140956

Ya-jun, Y., Bi-qin, D., Hong-xing, X., Xu-song, Z., Heong, K.L. and Zhong-xian, L., 2014. Susceptibility to insecticides and ecological fitness in resistant rice varieties of field Nilaparvata lugens Stål population free from insecticides in laboratory. Rice Sci., 21: 181-186. https://doi.org/10.1016/S1672-6308(13)60181-X

To share on other social networks, click on any share button. What are these?

Pakistan Journal of Zoology

October

Pakistan J. Zool., Vol. 56, Iss. 5, pp. 2001-2500

Featuring

Click here for more

Subscribe Today

Receive free updates on new articles, opportunities and benefits


Subscribe Unsubscribe